Canonical Allele Identifier: CA3031017
Gene: TACR3 HGNC NCBI

Linked Data

ClinVar Variation Id: 436938
ClinVar RCV Id: RCV000500874
dbSNP Id: rs376656496
ExAC: 4:104512837 C / T
gnomAD v2: 4-104512837-C-T
gnomAD v3: 4-103591680-C-T
gnomAD v4: 4-103591680-C-T
MyVariant Identifiers: chr4:g.104512837C>T (hg19) chr4:g.103591680C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.103591680C>T , CM000666.2:g.103591680C>T GRCh38
NC_000004.11:g.104512837C>T , CM000666.1:g.104512837C>T GRCh37
NC_000004.10:g.104732286C>T NCBI36
NG_023344.1:g.133137G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000304883.3:c.892G>A MANE Select ENSP00000303325.2:p.Val298Ile
ENST00000304883.2:c.892G>A ENSP00000303325.2:p.Val298Ile
NM_001059.2:c.892G>A NP_001050.1:p.Val298Ile
NM_001059.3:c.892G>A MANE Select NP_001050.1:p.Val298Ile
Search 100 bp 5'
Search 100 bp 3'